National Brain Research Centre, Manesar 122050, Haryana, India.
Mol Biol Rep. 2012 Sep;39(9):8695-9. doi: 10.1007/s11033-012-1726-5. Epub 2012 Jun 15.
Resistance of glioblastoma multiforme (GBM) to TNFα induced apoptosis is attributed to NFκB activation. As TNF-receptor family member CD40 regulates NFκB activation, we investigated the role of CD40 in NFκB activation in GBM. We observed elevated CD40 levels in human glioma samples as compared to the surrounding normal tissue. Treatment with TNFα elevated CD40 levels in glioma cells and inhibition of CD40 signaling failed to abrogate TNFα induced NFκΒ activity. While TNFα increased the interaction between TRAF2/6, IκBα, IKKα/β in the CD40 signalosome, the level of CD40 in the signalosome remained unaffected upon TNFα treatment. Interestingly, TNFα decreased the spatial localization of CD40 and increased TRAF2/6 co-localization with lipid raft marker Caveolin. As localization of CD40 signalosome in lipid raft is crucial for NFκB activation, TNFα mediated decreased clustering of CD40 in lipid rafts could have possibly contributed to its non-involvement in NFκB activation.
多形性胶质母细胞瘤(GBM)对 TNFα 诱导的细胞凋亡的抵抗归因于 NFκB 的激活。由于 TNF 受体家族成员 CD40 调节 NFκB 的激活,我们研究了 CD40 在 GBM 中 NFκB 激活中的作用。与周围正常组织相比,我们观察到人类脑肿瘤样本中 CD40 水平升高。TNFα 处理可上调胶质瘤细胞中的 CD40 水平,而抑制 CD40 信号转导不能消除 TNFα 诱导的 NFκB 活性。虽然 TNFα 增加了 TRAF2/6、IκBα、IKKα/β 在 CD40 信号体中的相互作用,但 TNFα 处理后信号体中的 CD40 水平没有变化。有趣的是,TNFα 降低了 CD40 的空间定位,增加了 TRAF2/6 与脂筏标记物 Caveolin 的共定位。由于 CD40 信号体在脂筏中的定位对于 NFκB 的激活至关重要,因此 TNFα 介导的 CD40 在脂筏中的聚集减少可能导致其不参与 NFκB 的激活。